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Effect of Tongluojiunao injection made from Sanqi (Radix Notogin- seng) and Zhizi (Fructus Gordenioe) on brain microvascular endothe- lial cells and astrocytes in an in vitro ischemic model
作者姓名:Weihong Li,  Xingguang Li,  Qinghong Du,  Feng Li,  Yuan zhu,  Yang Liu,  Jie Ma,  Liangqin Wan,  Fanghe Li,  Sai Zhang
作者单位:[1]School of PreclinicalMedicine, Beijing University of Chinese Medicine, Beijing100029, China; [2]Encephalopathy Center, Jiangsu Province Hospi-tal of Traditional Chinese Medicine, Nanjing 210029, China; [3]Medical Affairs, Novartis Pharmaceuticals (China),Beijing 100020, China
基金项目:the National Natural Science Foundation of China (No. 81273885): the Vascular-protecting Molecular Mechanism of Composition Compatibility in Gardenia and Panax Notoginseng Could be Explained by Integration of Cell Signaling Pathway Network; Collaborative Innovation Project of the Beijing University of Chinese Medicine: "Nauti- cal Traditional Chinese Medicine" Collaborative Innovation Center (No. 522/0100604299)
摘    要:OBJECTIVE: To explore the effect of Tongluojiunao injection(TLJN) prepared with Sanqi(Radix Notoginseng) and Zhizi(Fructus Gardeniae) on the interaction between brain microvascular endothelial cells(BMECs) and astrocytes in an in vitro ischemic model.METHODS: First, an in vitro model of cerebral ischemia in BMECs or astrocytes was established by oxygen-glucose deprivation(OGD). TLJN was used as a medicine of intervention. The OGD-injuredBMECs were cultured in various astrocyte-conditioned media. Cell activity, alkaline phosphatase(AKP) and γ-glutamyl transpeptidase(γ-GT) activity,interleukin-1 beta(IL-1β), and tumor necrosis factor alpha(TNF-α) content in BMECs were determined.Additionally, OGD-injured astrocytes were cultured in various BMEC-conditioned media. Cell activity, as well as expression of brain-derived neurotrophic factor(BDNF) and glial cell-derived neurotrophic factor(GDNF) in astrocytes, were detected.RESULTS: The results of paracrine signaling of normal BMECs or astrocytes showed a protective effect on each other: conditioned media from normal astrocytes improved cell viability, AKP, and γ-GT activity, and reduced IL-1β and TNF-α content of injured BMECs; conditioned media from normal BMECs improved cell viability and expression of BDNF and GDNF in injured astrocytes. However, once the BMECs or astrocytes were injured by OGD, the protective effect decreased or disappeared. The above-mentioned protective induction was effectively recovered by TLJN intervention.CONCLUSION: The therapeutic benefit of TLJN was achieved by recovering two-way induction between BMECs and astrocytes, enhancing activity of injured BMECs and astrocytes, stabilizing enzymatic barriers, promoting expression of neurotrophic factors, and inhibiting inflammatory cytokines.

关 键 词:脑微血管内皮细胞  星形胶质细胞  模型制作  脑缺血  胶质细胞源性神经营养因子  注射液  体外  Lial
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